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Pramipexole Dihydrochloride

NDC 69680-145 · Vitruvias Therapeutics, Inc.

Generic namePramipexole Dihydrochloride
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)PRAMIPEXOLE DIHYDROCHLORIDE
Strength.375 mg/1
Pharmacologic classDopamine Agonists [MoA], Nonergot Dopamine Agonist [EPC]
Marketing categoryANDA

Packages

69680-145-30 — 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-145-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65862-606 — Pramipexole Dihydrochloride, 65862-607 — Pramipexole Dihydrochloride, 65862-608 — Pramipexole Dihydrochloride, 65862-609 — Pramipexole Dihydrochloride, 68462-330 — Pramipexole dihydrochloride, 68462-331 — Pramipexole dihydrochloride, 68462-332 — Pramipexole dihydrochloride, 68462-333 — Pramipexole dihydrochloride, 68462-334 — Pramipexole dihydrochloride, 68462-627 — Pramipexole dihydrochloride, 69680-146 — Pramipexole Dihydrochloride, 71034-002 — Pramipexole Dihydrochloride, 71034-003 — Pramipexole Dihydrochloride, 71335-0584 — Pramipexole Dihydrochloride, 71335-1504 — Pramipexole Dihydrochloride, 71335-1537 — Pramipexole Dihydrochloride, 71335-1808 — Pramipexole Dihydrochloride, 71335-1877 — Pramipexole Dihydrochloride, 71335-2167 — Pramipexole Dihydrochloride, 72162-2569 — Pramipexole Dihydrochloride, +116 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.